tetradecyl palmitate
hexadecanoic acid, tetradecyl ester
 
Notes:
None found
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CAS Number: 4536-26-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 224-884-4
FDA UNII: 05918JMY6W
Nikkaji Web: J111.010A
MDL: MFCD00056206
XlogP3-AA: 14.10 (est)
Molecular Weight: 452.80660000
Formula: C30 H60 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
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Pubchem Patents: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 484.94 °C. @ 760.00 mm Hg (est)
Flash Point: 492.00 °F. TCC ( 255.50 °C. ) (est)
logP (o/w): 14.032 (est)
Soluble in:
 water, 3.259e-009 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Santa Cruz Biotechnology
For experimental / research use only.
Palmitic Acid Myristyl Ester
Sigma-Aldrich: Sigma
For experimental / research use only.
Myristyl palmitate ∼99%
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: information only not used for fragrances or flavors
Recommendation for tetradecyl palmitate usage levels up to:
 not for fragrance use.
 
Recommendation for tetradecyl palmitate flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA Substance Registry Services (TSCA): 4536-26-9
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 78294
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: nwg
 tetradecyl hexadecanoate
Chemidplus: 0004536269
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References:
 tetradecyl hexadecanoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 4536-26-9
Pubchem (cid): 78294
Pubchem (sid): 135033986
Pherobase: View
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
HMDB (The Human Metabolome Database): Search
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 hexadecanoic acid tetradecyl ester
 hexadecanoic acid, tetradecyl ester
 myristyl palmitate
 tetradecyl hexadecanoate
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Articles:
PubMed: Fatty acyl-CoA reductase and wax synthase from Euglena gracilis in the biosynthesis of medium-chain wax esters.
PubMed: Mediation of oviposition responses in the malaria mosquito Anopheles stephensi Liston by certain fatty acid esters.
PubMed: Microemulsions as transdermal drug delivery vehicles.
PubMed: Straightforward synthesis of two pairs of enantiomeric butenolides 3-tetradecyl- and 3-hexadecyl-5-methyl-2(5H)-furanone.
PubMed: Myristyl and palmityl acylation of pI 5.1 carboxylesterase from porcine intestine and liver.
PubMed: Acylation of monocyte and glomerular mesangial cell proteins. Myristyl acylation of the interleukin 1 precursors.
PubMed: Effects of acylcarnitine-transferase inhibitors on adenine nucleotide metabolism and ischemic tissue injury in isolated perfused rat heart.
PubMed: Myristyl and palmityl acylation of the insulin receptor.
PubMed: Comedogenicity of current therapeutic products, cosmetics, and ingredients in the rabbit ear.
PubMed: In vivo modification of retroviral gag gene-encoded polyproteins by myristic acid.
PubMed: Isolation, structural studies and chemical synthesis of a 'palmitone lipid' from Corynebacterium diphtheriae.
PubMed: ORIGIN OF PALMITIC ACID CARBON IN PALMITATES FORMED FROM HEXADECANE-1-C-14 AND TETRADECANE-1-C-14 BY MICROCOCCUS CERIFICANS.
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